{{Rsnum
|rsid=121907988
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PHGDH
|position=119742870
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PHGDH
}}{{omim
|id=606879
|rsnum=121907988
|variant=0002
}}{{ClinVar
|rsid=121907988
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=119742870
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=PHGDH:26227
|GENE_NAME=PHGDH
|GENE_ID=26227
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.119742870G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006623.3:c.1273G>A; 606879.0002
|CLNSIG=5
|CLNCUI=C1866174
|CLNDBN=Phosphoglycerate dehydrogenase deficiency
|Disease=Phosphoglycerate dehydrogenase deficiency
|CLNACC=RCV000004072.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1866174:601815
}}